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(3aS,8aR)-3,5-Bis-(4-chloro-phenyl)-1,7-diphenyl-8a-p-tolyl-3a,8a-dihydro-1H,7H-benzo[1,2-c;5,4-c']dipyrazole-4,8-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132782-90-2

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132782-90-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132782-90-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,7,8 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132782-90:
(8*1)+(7*3)+(6*2)+(5*7)+(4*8)+(3*2)+(2*9)+(1*0)=132
132 % 10 = 2
So 132782-90-2 is a valid CAS Registry Number.

132782-90-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (4aS,7aR)-3,5-bis(4-chlorophenyl)-1,7-diphenyl-7a-(p-tolyl)-7,7a-dihydropyrazolo[4,3-f]indazole-4,8(1H,4aH)-dione

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:132782-90-2 SDS

132782-90-2Downstream Products

132782-90-2Relevant academic research and scientific papers

1,3-Dipolar Cycloaddition Reactions of 1,4-Benzoquinones with Nitrilimines

Argyropoulos, N. G.,Mentzafos, D.,Terzis, A.

, p. 1983 - 1988 (2007/10/02)

The cycloaddition reactions of some aryl conjugated p-benzoquinones with nitrilimines were studied.Depending upon the reaction conditions mono- and/or bis- adducts were isolated only from carbon-carbon double bond.The structure determination was unequivocally established by an X-ray analysis carried out on a bis-adduct.The observed regio-, as well as site-selectivity was qualitatively correlated with frontier molecular orbitals of the reacting species.

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